The Rehabilitation of Atrophic Jaws Using Short Implants With Different Surface Characteristics
- Conditions
- PeriimplantitisOsseointegration Failure of Dental ImplantPeri-Implantation LossPeriodontal Bone LossGingival InflammationImplant Complication
- Interventions
- Device: implants placement
- Registration Number
- NCT05766878
- Lead Sponsor
- University of Foggia
- Brief Summary
The aim of the research is to evaluate the clinical outcome of short dental implants, characterized by a new macro-structural design and inserted in the upper or lower jaw in patients with reduced bone volume. The clinical outcomes will be compared for different surface treatments of implant neck and those of prosthetic components.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- healthy patients, with edentulous maxillary or mandibular ridge, requiring rehabilitation with two adjacent implants;
- at least 6 month after extraction;
- post-extractive implants;
- sites requiring bone regeneration or maxillary sinus lift;
- general health problems that contraindicate implant treatment.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description machined collar implants placement The arm will be constituted by healthy people, that need to be rehabilitated by dental implant placement. A short implant (length 6mm; diameter 4.3) will be inserted in an edentulous site. The implant will present a surface treated with double acid etching and traditional machined collar. A definitive transgingival standard machined abutment will be immediately screwed. Four months later, prosthetic procedures will start. anodized collar implants placement The arm will be constituted by healthy people, that need to be rehabilitated by dental implant placement. A short implant (length 6mm; diameter 4.3) will be inserted in an edentulous site. The implant will present a surface treated with double acid etching and anodized collar. A definitive transgingival anodized abutment will be immediately screwed. Four months later, prosthetic procedures will start.
- Primary Outcome Measures
Name Time Method Marginal Bone remodeling around the implant 0-4-12 months after implant placement The marginal bone remodeling will be evaluated by Radiographic examination. Periapical radiographs will be performed using paralleling technique with a Rinn-type positioner, customized for each patient at implant placement (T0), prosthetic restoration delivery (T1), and after 12 months (T2).Peri-implant bone levels will be measured at each time point as the linear distance (in mm) between implant platform and bone crest at mesial and distal aspects of each implant. A positive value will be assigned if the bone crest is coronal to the implant platform, whereas a negative value will be assigned if the first bone-to implant contact is apical to the implant platform. All measurements will be performed by two examiners, using measuring software (Image J). Each measurement will be performed three times at three different points.
- Secondary Outcome Measures
Name Time Method Periodontal indexes: Probing Depth The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement. Probing Depth (PD) will be calculated as the distance (in mm) from the gingival peri-implant margin to the bottom of the peri-implant pocket.
Implant Stability evaluation 0-4 months. Primary and secondary implant stability will be measured with resonance frequency analysis (RFA) and subsequently expressed as an implant stability quotient (ISQ). The Implant stability will be measured immediately after placement (T0) and at 4 months (T1) after placement, when the osseointegration is supposed to take place.
Suppuration on probing The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement. Suppuration on probing (SUP) will be scored dichotomously (Yes/No). The probing will be performed on 6 sites around the implant (3 buccal and 3 palatal/lingual) and appearance of pus or purulent exudate will be registered (Yes). The final score will be expressed as number of suppurative sites/total of probed sites (%)
Bleeding on Probing The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement. Bleeding on probing (BoP) will be scored dichotomously (Yes/No). The probing will be performed on 6 sites around the implant (3 buccal and 3 palatal/lingual) and appearance of blood will be registered (Yes). The final score will be expressed as number of bleeding sites/total of probed sites (%)
Plaque index of peri-implant tissues The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement. Plaque Index (PI) will be calculated by assigning a binary score to each surface (1= plaque present, 0 = plaque absent).
Trial Locations
- Locations (3)
Clinica Odontoiatrica, University of Foggia
🇮🇹Foggia, Italy
University of Genoa
🇮🇹Genova, Italy
University of Turin
🇮🇹Torino, Italy